US11380847B2 - Thermally activated delayed fluorescent material, preparation method thereof, and electroluminescent device - Google Patents

Thermally activated delayed fluorescent material, preparation method thereof, and electroluminescent device Download PDF

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US11380847B2
US11380847B2 US16/641,291 US202016641291A US11380847B2 US 11380847 B2 US11380847 B2 US 11380847B2 US 202016641291 A US202016641291 A US 202016641291A US 11380847 B2 US11380847 B2 US 11380847B2
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thermally activated
activated delayed
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fluorescent material
delayed fluorescent
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Jiajia Luo
Shuxing YAN
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Wuhan China Star Optoelectronics Semiconductor Display Technology Co Ltd
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    • C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
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    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
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    • H10K50/00—Organic light-emitting devices
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    • H10K50/14—Carrier transporting layers
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    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/17—Carrier injection layers

Definitions

  • the present invention relates to a field of display technology, and particularly to a thermally activated delayed fluorescence (TADF) material, a preparation method thereof, and an electroluminescent device.
  • TADF thermally activated delayed fluorescence
  • OLEDs organic light-emitting diodes
  • a conventional OLED display device generally includes a substrate, an anode disposed on the substrate, an organic light-emitting layer disposed on the anode, an electron transport layer disposed on the organic light-emitting layer, and a cathode disposed on the electron transport layer.
  • holes from the anode and electrons from the cathode are emitted to the organic light-emitting layer, and these electrons and holes are combined to generate an excited electron-hole pairs, and the excited electron-hole pairs are converted from an excited state to a ground state to achieve light-emitting.
  • a dominant luminescent guest material is critical.
  • Guest luminescent materials for early OLEDs are fluorescent materials. Because the ratio of excitons in a singlet energy state and excitons in a triplet energy state in the OLED is 1:3, the theoretical internal quantum efficiency (IQE) of fluorescent-based OLEDs can merely reach 25%, thus considerably limiting the application of fluorescent electroluminescent devices.
  • Heavy metal complex phosphorescent materials can achieve 100% IQE by using the excitons in the singlet energy state and the excitons in the triplet energy state due to a spin-orbit coupling of heavy atoms.
  • heavy metals commonly employed are precious metals, such as Ir, Pt, and the like, and the heavy metal complex phosphorescent materials have yet to be developed in fields of blue light materials.
  • pure organic thermally activated delayed fluorescence (TADF) materials can have a small minimum energy state difference (A EST) between the singlet energy state and the triplet energy state, so that the excitons in the triplet energy state can be returned by reverse intersystem crossing (RISC) back to the singlet energy state, then to a ground state by a radiation transition to emit light, and thereby simultaneously use the excitons in the singlet energy state and in the triplet energy state, and 100% IQE may also be achieved.
  • a EST energy state difference
  • RISC reverse intersystem crossing
  • TADF materials For TADF materials, fast reverse intersystem-crossing (kRISC) and high photoluminescence quantum yield (PLQY) are necessary conditions for preparing high-efficiency OLEDs. At present, TADF materials with the above conditions are still relatively scarce compared to heavy metal Ir complexes. Because TADF materials have very wide spectrums and exciton lifetimes of microseconds, their applications in mass-produced device structures are greatly limited.
  • kRISC fast reverse intersystem-crossing
  • PLQY photoluminescence quantum yield
  • TADF thermally activated delayed fluorescence
  • An object of the present invention is to provide a thermally activated delayed fluorescence (TADF) material as a host of a green light-emitting guest, and using 100% of the internal quantum efficiency of the TADF material, a fluorescent device can achieve efficiency of a phosphorescent device, while solving the problems of excessively broad spectrum and long exciton life, thereby overcoming the problem of color gamut difference when directly using the TADF light-emitting material, such that blockade of UDC patents in phosphorescent heavy metal complex can be broken, and cost is significantly reduced. Therefore, a series of high-performance TADF organic light-emitting diodes (OLEDs) can be prepared by using the light-emitting materials provided by the present invention.
  • TADF thermally activated delayed fluorescence
  • the present invention provides a thermally activated delayed fluorescence (TADF) material, which includes a compound composed of an acceptor A and a donor D, the compound having a following structural formula of Formula 1: D-A Formula 1,
  • TADF thermally activated delayed fluorescence
  • receptor A is selected from any one of following structural formulas:
  • the present invention also provides a method of preparing a thermally activated delayed fluorescent material, including the following steps:
  • Step S 1 performing a reaction between a compound of A-X and a compound of D-H in a solution containing an alkali with catalyst at a first temperature for a first duration to obtain a reaction solution, wherein X is a halogen, A is selected from any one of the following structural formulas:
  • Step S 2 cooling the reaction solution to a second temperature to obtain a mixture
  • Step S 3 separating the thermally activated delayed fluorescent material from the mixture, wherein the compound is composed of an acceptor A and a donor D, and the compound has a following structural formula of Formula 1: D-A Formula 1.
  • the first temperature is 120° C.
  • the first duration is 48 hours.
  • the second temperature is room temperature.
  • the solution containing the alkali is toluene
  • the alkali is sodium tert-butoxide
  • the catalyst includes acetic acid palladium and tri-tert-butylphosphine tetrafluoroborate.
  • the step S 2 further includes extracting the reaction solution several times with dichloromethane and combining organic extracts to obtain the mixture.
  • the separating is performed by column chromatography with an eluent of methylene chloride and n-hexane in a volume ratio of 1:1.
  • the step S 1 is performed under an inert environment.
  • the present invention further provides an electroluminescent device, including: a base layer; a hole injection layer disposed on the base layer; a hole transport layer disposed on the hole injection layer; a light-emitting layer disposed on the hole transport layer; an electron transport layer disposed on the light-emitting layer; and a cathode layer disposed on the electron transport layer, wherein the light-emitting layer includes the thermally activated delayed fluorescent material according to the present invention.
  • the base layer is made of a material including ITO;
  • the injection layer is made of a material including 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexaazabenzophenanthrene;
  • the hole transport layer is made of a material including 4,4′,4′′-tris(carbazole-9-yl)triphenylamine;
  • the electron transport layer is made of a material including 1,3,5-tris(3-(3-pyridyl)phenyl)benzene(Tm3PyPB);
  • the cathode layer is made of a material including lithium fluoride and aluminum.
  • An object of the present invention is to provide a thermally activated delayed fluorescence (TADF) material as a host of a green light-emitting guest, and using 100% of the internal quantum efficiency of the TADF material, a fluorescent device can achieve efficiency of a phosphorescent device, while solving the problems of excessively broad spectrum and long exciton life, thereby overcoming the problem of color gamut difference when directly using the TADF light-emitting material, such that blockade of UDC patents in phosphorescent heavy metal complex can be broken, and cost is significantly reduced. Therefore, a series of high-performance TADF organic light-emitting diodes (OLEDs) can be prepared by using the light-emitting materials provided by the present invention.
  • TADF thermally activated delayed fluorescence
  • FIG. 1 is a flowchart of a method of preparing a thermally activated delayed fluorescence (TADF) material according to an embodiment of the present invention.
  • TADF thermally activated delayed fluorescence
  • FIG. 2 is a fluorescence emission spectrum diagram of Compound 1, Compound 2, and Compound 3 in Examples 1, 2, and 3 of the present invention.
  • FIG. 3 is a schematic structural diagram of an electroluminescent device according to an embodiment of the present invention.
  • An embodiment of the present invention provides a thermally activated delayed fluorescence (TADF) material as a host of a green light-emitting guest, and using 100% of the internal quantum efficiency of the TADF material, a fluorescent device can achieve efficiency of a phosphorescent device, while solving the problems of excessively broad spectrum and long exciton life, thereby overcoming the problem of color gamut difference when directly using the TADF light-emitting material, such that blockade of UDC patents in phosphorescent heavy metal complex can be broken, and cost is significantly reduced. Therefore, a series of high-performance TADF organic light-emitting diodes (OLEDs) can be prepared by using the light-emitting materials provided by the present invention.
  • TADF thermally activated delayed fluorescence
  • the present invention provides a thermally activated delayed fluorescence (TADF) material, which includes a compound composed of an acceptor A and a donor D, the compound having a following structural formula of Formula 1: D-A Formula 1,
  • TADF thermally activated delayed fluorescence
  • receptor A is selected from any one of following structural formulas:
  • FIG. 1 is a flowchart of a method of preparing a thermally activated delayed fluorescence (TADF) material according to an embodiment of the present invention. As shown in FIG. 1 , the present invention also provides a method of preparing a thermally activated delayed fluorescence (TADF) material, including the following steps:
  • Step S 1 performing a reaction between a compound of A-X and a compound of D-H in a solution containing an alkali with catalyst at a first temperature for a first duration to obtain a reaction solution, wherein X is a halogen, A is selected from any one of the following structural formulas:
  • Step S 2 cooling the reaction solution to a second temperature to obtain a mixture
  • Step S 3 separating the thermally activated delayed fluorescent material from the mixture, wherein the compound is composed of an acceptor A and a donor D, and the compound has a following structural formula of Formula 1: D-A Formula 1.
  • the first temperature is 120° C.
  • the first duration is 48 hours.
  • the second temperature is room temperature.
  • the solution containing the alkali is toluene
  • the alkali is sodium tert-butoxide
  • the catalyst includes acetic acid palladium and tri-tert-butylphosphine tetrafluoroborate.
  • the step S 2 further includes extracting the reaction solution several times with dichloromethane and combining organic extracts to obtain the mixture.
  • the separating is performed by column chromatography with an eluent of methylene chloride and n-hexane in a volume ratio of 1:1.
  • the step S 1 is performed under an inert environment.
  • the present invention further provides an electroluminescent device, including: a base layer; a hole injection layer disposed on the base layer; a hole transport layer disposed on the hole injection layer; a light-emitting layer disposed on the hole transport layer; an electron transport layer disposed on the light-emitting layer; and a cathode layer disposed on the electron transport layer, wherein the light-emitting layer includes the thermally activated delayed fluorescent material according to the present invention.
  • the base layer is made of a material including ITO;
  • the injection layer is made of a material including 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexaazabenzophenanthrene;
  • the hole transport layer is made of a material including 4,4′,4′′-tris(carbazole-9-yl)triphenylamine;
  • the electron transport layer is made of a material including 1,3,5-tris(3-(3-pyridyl)phenyl)benzene(Tm3PyPB);
  • the cathode layer is made of a material including lithium fluoride and aluminum.
  • the target thermally activated delayed fluorescence (TADF) material to be synthesized includes Compound 1 having the following structural formula:
  • Raw Material 1 (1.75 g, 5 mmol), phenoxazine (1.10 g, 6 mmol), palladium acetate (45 mg, 0.2 mmol), and tri-tert-butylphosphine tetrafluoroborate (0.17 g, 0.6 mmol) were added to a 100 mL two-necked flask, then sodium tert-butylate (NaOtBu) (0.58 g, 6 mmol) was added thereto in a glove box, and then 40 mL of dehydrated and deoxygenated toluene was injected therein under an argon atmosphere to perform a reaction at 120° C. for 48 hours, followed by cooling the reaction solution to room temperature.
  • NaOtBu sodium tert-butylate
  • the target thermally activated delayed fluorescence (TADF) material to be synthesized includes Compound 2 having the following structural formula:
  • Raw Material 2 (1.75 g, 5 mmol), phenoxazine (1.10 g, 6 mmol), palladium acetate (45 mg, 0.2 mmol), and tri-tert-butylphosphine tetrafluoroborate (0.17 g, 0.6 mmol) were added to a 100 mL two-necked flask, then sodium tert-butylate (NaOtBu) (0.58 g, 6 mmol) was added thereto in a glove box, and then 40 mL of dehydrated and deoxygenated toluene was injected therein under an argon atmosphere to perform a reaction at 120° C. for 48 hours, followed by cooling the reaction solution to room temperature.
  • NaOtBu sodium tert-butylate
  • the target thermally activated delayed fluorescence (TADF) material to be synthesized includes Compound 3 having the following structural formula:
  • Raw Material 3 (1.75 g, 5 mmol), phenoxazine (1.10 g, 6 mmol), palladium acetate (45 mg, 0.2 mmol), and tri-tert-butylphosphine tetrafluoroborate (0.17 g, 0.6 mmol) were added to a 100 mL two-necked flask, then sodium tert-butylate (NaOtBu) (0.58 g, 6 mmol) was added thereto in a glove box, and then 40 mL of dehydrated and deoxygenated toluene was injected therein under an argon atmosphere to perform a reaction at 120° C. for 48 hours, followed by cooling the reaction solution to room temperature.
  • NaOtBu sodium tert-butylate
  • reaction solution was poured into 200 mL of ice-water, followed by extraction three times with dichloromethane, and the organic extracts were combined, and separated and purified using silica gel column chromatography (dichloromethane:n-hexane, v:v, 1:1), such that 1.0 g of a blue-white powder was obtained with a yield of 44%.
  • PL peak is the photoluminescence peak
  • S 1 is the lowest singlet energy level
  • T1 is the lowest triplet energy level
  • ⁇ EST is the energy level difference between the lowest singlet energy level and the lowest triplet energy level
  • HOMO is the highest occupied molecular orbital
  • LUMO is the lowest unoccupied molecular orbital.
  • an embodiment of the present invention also provides an electroluminescent device including the above-described thermally activated delayed fluorescent (TADF) material.
  • TADF thermally activated delayed fluorescent
  • the electroluminescent device 100 includes: a substrate layer 1 ; a hole injection layer 2 disposed on the substrate layer 1 ; a hole transport layer 3 disposed on the hole injection layer 2 ; a light-emitting layer 4 disposed on the hole transport layer 3 ; an electron transport layer 5 disposed on the light-emitting layer 4 ; and a cathode layer 6 disposed on the electron transport layer 5 , wherein the light-emitting layer 4 includes the thermally activated delayed fluorescent (TADF) material.
  • TADF thermally activated delayed fluorescent
  • the base layer is made of material including ITO; the hole injection layer is made of material including 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexaazatriphenylene; the hole transport layer 3 is made of material including 44,4′,4′′-Tris(carbazol-9-yl)-triphenylamine (TCTA); the electron transport layer 5 is made of material including 1,3,5-tris(3-(3-pyridyl)phenyl)benzene (Tm3PyPB); and the cathode layer is made of material including lithium fluoride and aluminum.
  • Compound 1, Compound 2, and Compound 3 are used as the light-emitting layers 4 to manufacture Device 100 , Device 200 , and Device 300 , respectively, and performance of Device 100 , Device 200 , and Device 300 was measured.
  • a thickness of each of the base layer 1 and the hole injection layer 2 is 2 nm
  • a thickness of the hole transport layer 3 is 35 nm.
  • the light-emitting layer 4 of Device 100 , Device 200 , and Device 300 includes 7% of Compound 1, Compound 2, and Compound 3, respectively, and has a thickness of 40 nm.
  • a thickness of the electron transport layer 5 is 40 nm
  • a thickness of lithium fluoride is 1 nm
  • a thickness of aluminum is 100 nm.
  • the current-brightness-voltage characteristics of Device 100 , Device 200 , and Device 300 were further measured by a Keithley source measurement system (Keithley 2400 Sourcemeter, Keithley 2000 Currentmeter) with a calibrated silicon photodiode.
  • the electroluminescence spectrum was measured by a French JY SPEX CCD3000 spectrometer. All measurements were conducted at room temperature under ambient atmosphere.
  • the performance data of Device 100 , Device 200 , and Device 300 is shown in Table 2 below, and Device 100 , Device 200 , and Device 300 meet the performance requirements.
  • an embodiment of the present invention provides a thermally activated delayed fluorescence (TADF) material as a host of a green light-emitting guest, and using 100% of the internal quantum efficiency of the TADF material, a fluorescent device can achieve efficiency of a phosphorescent device, while solving the problems of excessively broad spectrum and long exciton life, thereby overcoming the problem of color gamut difference when directly using the TADF light-emitting material, such that blockade of UDC patents in phosphorescent heavy metal complex can be broken, and cost is significantly reduced. Therefore, a series of high-performance TADF organic light-emitting diodes (OLEDs) can be prepared by using the light-emitting materials provided by the present invention.
  • TADF thermally activated delayed fluorescence

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Abstract

The present invention provides at thermally activated delayed fluorescent material, including a compound composed of an acceptor A and a donor D, the compound having a following structural formula of Formula 1:
D-A  Formula 1,
    • wherein the receptor A is selected from any one of following structural formulas:
Figure US11380847-20220705-C00001
    • and the donor D has a following structural formula:
Figure US11380847-20220705-C00002

Description

CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a U.S. National Phase of International PCT Application No. PCT/CN2020/071737 filed Jan. 13, 2020, which claims the benefit of Chinese Patent Application Serial No. 201911178329.6 filed Nov. 27, 2019, the contents of each application are incorporated herein by reference in their entirety.
BACKGROUND OF INVENTION Field of Invention
The present invention relates to a field of display technology, and particularly to a thermally activated delayed fluorescence (TADF) material, a preparation method thereof, and an electroluminescent device.
Description of Prior Art
It is known that organic light-emitting diodes (OLEDs) have attracted attention from many researchers, due to their huge application prospects and advantages, such as self-illumination without the need for a backlight, high luminous efficiency, wide viewing angles, fast response speed, a large temperature adaptation range, relatively simple production and processing techniques, low driving voltage, low energy consumption, lightness, thinness, flexibility, and so on.
A conventional OLED display device generally includes a substrate, an anode disposed on the substrate, an organic light-emitting layer disposed on the anode, an electron transport layer disposed on the organic light-emitting layer, and a cathode disposed on the electron transport layer. During operation, holes from the anode and electrons from the cathode are emitted to the organic light-emitting layer, and these electrons and holes are combined to generate an excited electron-hole pairs, and the excited electron-hole pairs are converted from an excited state to a ground state to achieve light-emitting.
In OLEDs, a dominant luminescent guest material is critical. Guest luminescent materials for early OLEDs are fluorescent materials. Because the ratio of excitons in a singlet energy state and excitons in a triplet energy state in the OLED is 1:3, the theoretical internal quantum efficiency (IQE) of fluorescent-based OLEDs can merely reach 25%, thus considerably limiting the application of fluorescent electroluminescent devices. Heavy metal complex phosphorescent materials can achieve 100% IQE by using the excitons in the singlet energy state and the excitons in the triplet energy state due to a spin-orbit coupling of heavy atoms. However, heavy metals commonly employed are precious metals, such as Ir, Pt, and the like, and the heavy metal complex phosphorescent materials have yet to be developed in fields of blue light materials.
Through a molecular design, pure organic thermally activated delayed fluorescence (TADF) materials can have a small minimum energy state difference (A EST) between the singlet energy state and the triplet energy state, so that the excitons in the triplet energy state can be returned by reverse intersystem crossing (RISC) back to the singlet energy state, then to a ground state by a radiation transition to emit light, and thereby simultaneously use the excitons in the singlet energy state and in the triplet energy state, and 100% IQE may also be achieved.
For TADF materials, fast reverse intersystem-crossing (kRISC) and high photoluminescence quantum yield (PLQY) are necessary conditions for preparing high-efficiency OLEDs. At present, TADF materials with the above conditions are still relatively scarce compared to heavy metal Ir complexes. Because TADF materials have very wide spectrums and exciton lifetimes of microseconds, their applications in mass-produced device structures are greatly limited.
In view of above, there is an urgent need to develop a thermally activated delayed fluorescence (TADF) material as a host of a green light-emitting guest. Using 100% of the internal quantum efficiency of the TADF material, a fluorescent device can achieve efficiency of a phosphorescent device, while solving the problems of excessively broad spectrum and long exciton life, such that an effective path to break blockade of UDC patents in phosphorescent heavy metal complex can be achieved.
SUMMARY OF INVENTION
An object of the present invention is to provide a thermally activated delayed fluorescence (TADF) material as a host of a green light-emitting guest, and using 100% of the internal quantum efficiency of the TADF material, a fluorescent device can achieve efficiency of a phosphorescent device, while solving the problems of excessively broad spectrum and long exciton life, thereby overcoming the problem of color gamut difference when directly using the TADF light-emitting material, such that blockade of UDC patents in phosphorescent heavy metal complex can be broken, and cost is significantly reduced. Therefore, a series of high-performance TADF organic light-emitting diodes (OLEDs) can be prepared by using the light-emitting materials provided by the present invention.
In order to achieve the above object, the present invention provides a thermally activated delayed fluorescence (TADF) material, which includes a compound composed of an acceptor A and a donor D, the compound having a following structural formula of Formula 1:
D-A  Formula 1,
wherein the receptor A is selected from any one of following structural formulas:
Figure US11380847-20220705-C00003
and the donor D has a following structural formula:
Figure US11380847-20220705-C00004
The present invention also provides a method of preparing a thermally activated delayed fluorescent material, including the following steps:
Step S1: performing a reaction between a compound of A-X and a compound of D-H in a solution containing an alkali with catalyst at a first temperature for a first duration to obtain a reaction solution, wherein X is a halogen, A is selected from any one of the following structural formulas:
Figure US11380847-20220705-C00005
and D has a following structural formula:
Figure US11380847-20220705-C00006
Step S2: cooling the reaction solution to a second temperature to obtain a mixture; and
Step S3: separating the thermally activated delayed fluorescent material from the mixture, wherein the compound is composed of an acceptor A and a donor D, and the compound has a following structural formula of Formula 1:
D-A  Formula 1.
According to an embodiment of the present invention, the first temperature is 120° C., and the first duration is 48 hours.
According to an embodiment of the present invention, the second temperature is room temperature.
According to an embodiment of the present invention, in the step S1, the solution containing the alkali is toluene, the alkali is sodium tert-butoxide, and the catalyst includes acetic acid palladium and tri-tert-butylphosphine tetrafluoroborate.
According to an embodiment of the present invention, the step S2 further includes extracting the reaction solution several times with dichloromethane and combining organic extracts to obtain the mixture.
According to an embodiment of the present invention, in the step S3, the separating is performed by column chromatography with an eluent of methylene chloride and n-hexane in a volume ratio of 1:1.
According to an embodiment of the present invention, the step S1 is performed under an inert environment.
The present invention further provides an electroluminescent device, including: a base layer; a hole injection layer disposed on the base layer; a hole transport layer disposed on the hole injection layer; a light-emitting layer disposed on the hole transport layer; an electron transport layer disposed on the light-emitting layer; and a cathode layer disposed on the electron transport layer, wherein the light-emitting layer includes the thermally activated delayed fluorescent material according to the present invention.
According to an embodiment of the present invention, the base layer is made of a material including ITO; the injection layer is made of a material including 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexaazabenzophenanthrene; the hole transport layer is made of a material including 4,4′,4″-tris(carbazole-9-yl)triphenylamine; the electron transport layer is made of a material including 1,3,5-tris(3-(3-pyridyl)phenyl)benzene(Tm3PyPB); and the cathode layer is made of a material including lithium fluoride and aluminum.
An object of the present invention is to provide a thermally activated delayed fluorescence (TADF) material as a host of a green light-emitting guest, and using 100% of the internal quantum efficiency of the TADF material, a fluorescent device can achieve efficiency of a phosphorescent device, while solving the problems of excessively broad spectrum and long exciton life, thereby overcoming the problem of color gamut difference when directly using the TADF light-emitting material, such that blockade of UDC patents in phosphorescent heavy metal complex can be broken, and cost is significantly reduced. Therefore, a series of high-performance TADF organic light-emitting diodes (OLEDs) can be prepared by using the light-emitting materials provided by the present invention.
BRIEF DESCRIPTION OF DRAWINGS
In order to more clearly illustrate the embodiments or the technical solutions of the existing art, the drawings illustrating the embodiments or the existing art will be briefly described below. Obviously, the drawings in the following description merely illustrate some embodiments of the present invention. Other drawings may also be obtained by those skilled in the art according to these figures without paying creative work.
FIG. 1 is a flowchart of a method of preparing a thermally activated delayed fluorescence (TADF) material according to an embodiment of the present invention.
FIG. 2 is a fluorescence emission spectrum diagram of Compound 1, Compound 2, and Compound 3 in Examples 1, 2, and 3 of the present invention.
FIG. 3 is a schematic structural diagram of an electroluminescent device according to an embodiment of the present invention.
 DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
In order to make the above content of the present invention more comprehensible, preferred embodiments are described in detail below with detailed description in conjunction with the accompanying drawings.
An embodiment of the present invention provides a thermally activated delayed fluorescence (TADF) material as a host of a green light-emitting guest, and using 100% of the internal quantum efficiency of the TADF material, a fluorescent device can achieve efficiency of a phosphorescent device, while solving the problems of excessively broad spectrum and long exciton life, thereby overcoming the problem of color gamut difference when directly using the TADF light-emitting material, such that blockade of UDC patents in phosphorescent heavy metal complex can be broken, and cost is significantly reduced. Therefore, a series of high-performance TADF organic light-emitting diodes (OLEDs) can be prepared by using the light-emitting materials provided by the present invention.
In order to achieve the above object, the present invention provides a thermally activated delayed fluorescence (TADF) material, which includes a compound composed of an acceptor A and a donor D, the compound having a following structural formula of Formula 1:
D-A  Formula 1,
wherein the receptor A is selected from any one of following structural formulas:
Figure US11380847-20220705-C00007
and the donor D has a following structural formula:
Figure US11380847-20220705-C00008
Referring to FIG. 1, FIG. 1 is a flowchart of a method of preparing a thermally activated delayed fluorescence (TADF) material according to an embodiment of the present invention. As shown in FIG. 1, the present invention also provides a method of preparing a thermally activated delayed fluorescence (TADF) material, including the following steps:
Step S1: performing a reaction between a compound of A-X and a compound of D-H in a solution containing an alkali with catalyst at a first temperature for a first duration to obtain a reaction solution, wherein X is a halogen, A is selected from any one of the following structural formulas:
Figure US11380847-20220705-C00009
and D has a following structural formula:
Figure US11380847-20220705-C00010
Step S2: cooling the reaction solution to a second temperature to obtain a mixture; and
Step S3: separating the thermally activated delayed fluorescent material from the mixture, wherein the compound is composed of an acceptor A and a donor D, and the compound has a following structural formula of Formula 1:
D-A  Formula 1.
According to an embodiment of the present invention, the first temperature is 120° C., and the first duration is 48 hours.
According to an embodiment of the present invention, the second temperature is room temperature.
According to an embodiment of the present invention, in the step S1, the solution containing the alkali is toluene, the alkali is sodium tert-butoxide, and the catalyst includes acetic acid palladium and tri-tert-butylphosphine tetrafluoroborate.
According to an embodiment of the present invention, the step S2 further includes extracting the reaction solution several times with dichloromethane and combining organic extracts to obtain the mixture.
According to an embodiment of the present invention, in the step S3, the separating is performed by column chromatography with an eluent of methylene chloride and n-hexane in a volume ratio of 1:1.
According to an embodiment of the present invention, the step S1 is performed under an inert environment.
The present invention further provides an electroluminescent device, including: a base layer; a hole injection layer disposed on the base layer; a hole transport layer disposed on the hole injection layer; a light-emitting layer disposed on the hole transport layer; an electron transport layer disposed on the light-emitting layer; and a cathode layer disposed on the electron transport layer, wherein the light-emitting layer includes the thermally activated delayed fluorescent material according to the present invention.
According to an embodiment of the present invention, the base layer is made of a material including ITO; the injection layer is made of a material including 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexaazabenzophenanthrene; the hole transport layer is made of a material including 4,4′,4″-tris(carbazole-9-yl)triphenylamine; the electron transport layer is made of a material including 1,3,5-tris(3-(3-pyridyl)phenyl)benzene(Tm3PyPB); and the cathode layer is made of a material including lithium fluoride and aluminum.
Example 1
In a specific Example 1 of the present invention, the target thermally activated delayed fluorescence (TADF) material to be synthesized includes Compound 1 having the following structural formula:
Figure US11380847-20220705-C00011
The compound 1 is synthesized by the following Reaction Scheme 1:
Figure US11380847-20220705-C00012
Detailed synthetic steps of Compound 1 are as follows:
Raw Material 1 (1.75 g, 5 mmol), phenoxazine (1.10 g, 6 mmol), palladium acetate (45 mg, 0.2 mmol), and tri-tert-butylphosphine tetrafluoroborate (0.17 g, 0.6 mmol) were added to a 100 mL two-necked flask, then sodium tert-butylate (NaOtBu) (0.58 g, 6 mmol) was added thereto in a glove box, and then 40 mL of dehydrated and deoxygenated toluene was injected therein under an argon atmosphere to perform a reaction at 120° C. for 48 hours, followed by cooling the reaction solution to room temperature. After that, the reaction solution was poured into 200 mL of ice-water, followed by extraction three times with dichloromethane, and the organic extracts were combined, and separated and purified using silica gel column chromatography (dichloromethane:n-hexane, v:v, 1:1), such that 1.8 g of a blue-white powder was obtained with a yield of 79%. 1H NMR (300 MHz, CD2Cl2, δ): 7.71 (d, J=7.2 Hz, 2H), 7.14 (d, J=6.9 Hz, 2H), 7.08 (d, J=6.6 Hz, 2H), 7.06-6.93 (m, 6H). MS (EI) m/z: [M]+ calcd for C25H12F5NO2, 453.08; found, 453.00.
Example 2
In a specific Example 2 of the present invention, the target thermally activated delayed fluorescence (TADF) material to be synthesized includes Compound 2 having the following structural formula:
Figure US11380847-20220705-C00013
The compound 1 is synthesized by the following Reaction Scheme 2:
Figure US11380847-20220705-C00014
Detailed synthetic steps of Compound 2 are as follows:
Raw Material 2 (1.75 g, 5 mmol), phenoxazine (1.10 g, 6 mmol), palladium acetate (45 mg, 0.2 mmol), and tri-tert-butylphosphine tetrafluoroborate (0.17 g, 0.6 mmol) were added to a 100 mL two-necked flask, then sodium tert-butylate (NaOtBu) (0.58 g, 6 mmol) was added thereto in a glove box, and then 40 mL of dehydrated and deoxygenated toluene was injected therein under an argon atmosphere to perform a reaction at 120° C. for 48 hours, followed by cooling the reaction solution to room temperature. After that the reaction solution was poured into 200 mL of ice-water, followed by extraction three times with dichloromethane, and the organic extracts were combined, and separated and purified using silica gel column chromatography (dichloromethane:n-hexane, v:v, 1:1), such that 1.6 g of a blue-white powder was obtained with a yield of 70%. 1H NMR (300 MHz, CD2Cl2, δ): 7.45 (s, 1H), 7.40-7.27 (m, 3H), 7.14 (d, J=6.6 Hz, 2H), 7.06-6.93 (m, 6H). MS (EI) m/z: [M]+ calcd for C25H12F5NO2, 453.08; found, 453.03.
Example 3
In a specific Example 3 of the present invention, the target thermally activated delayed fluorescence (TADF) material to be synthesized includes Compound 3 having the following structural formula:
Figure US11380847-20220705-C00015
The compound 1 is synthesized by the following Reaction Scheme 3:
Figure US11380847-20220705-C00016
Detailed synthetic steps of Compound 3 are as follows:
Raw Material 3 (1.75 g, 5 mmol), phenoxazine (1.10 g, 6 mmol), palladium acetate (45 mg, 0.2 mmol), and tri-tert-butylphosphine tetrafluoroborate (0.17 g, 0.6 mmol) were added to a 100 mL two-necked flask, then sodium tert-butylate (NaOtBu) (0.58 g, 6 mmol) was added thereto in a glove box, and then 40 mL of dehydrated and deoxygenated toluene was injected therein under an argon atmosphere to perform a reaction at 120° C. for 48 hours, followed by cooling the reaction solution to room temperature. After that the reaction solution was poured into 200 mL of ice-water, followed by extraction three times with dichloromethane, and the organic extracts were combined, and separated and purified using silica gel column chromatography (dichloromethane:n-hexane, v:v, 1:1), such that 1.0 g of a blue-white powder was obtained with a yield of 44%. 1H NMR (300 MHz, CD2Cl2, δ): 7.70 (d, J=6.3 Hz, 1H), 7.48 (t, J=6.9 Hz, 1H), 7.28 (t, J=6.9 Hz, 1H), 7.18 (t, J=7.2 Hz, 1H), 7.14 (d, J=6.6 Hz, 2H), 7.06-6.93 (m, 6H). MS (EI) m/z: [M]+ calcd for C25H12F5NO2, 453.08; found, 453.01.
Specifically, Compound 1, Compound 2, and Compound 3 are analyzed, and the fluorescence emission spectrum of Compound 1, Compound 2, and Compound 3 as a pure film is shown in FIG. 2. The lowest singlet state (S1) and lowest triplet energy level (T1) of Compound 1, Compound 2, and Compound 3 were calculated based on B3LYP theory, and the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) were detected. The obtained electrochemical energy is shown in Table 1 below:
TABLE 1
PL Peak S1 T1 EST HOMO LUMO
(nm) (eV) (eV) (eV) (eV) (eV)
Compound 1 531 2.34 2.30 0.04 −5.42 −2.28
Compound 2 542 2.29 2.28 0.01 −5.41 −2.28
Compound 3 549 2.26 2.24 0.02 −5.44 −2.28
PL peak is the photoluminescence peak, S1 is the lowest singlet energy level, T1 is the lowest triplet energy level, ΔEST is the energy level difference between the lowest singlet energy level and the lowest triplet energy level, HOMO is the highest occupied molecular orbital, and LUMO is the lowest unoccupied molecular orbital.
As can be known from FIG. 2 and Table 1, Compound 1, Compound 2, and Compound 3 of Example 1, Example 2, and Example 3 of the present invention satisfy the performance requirements.
Furthermore, an embodiment of the present invention also provides an electroluminescent device including the above-described thermally activated delayed fluorescent (TADF) material.
Referring to FIG. 3, in particular, the electroluminescent device 100 includes: a substrate layer 1; a hole injection layer 2 disposed on the substrate layer 1; a hole transport layer 3 disposed on the hole injection layer 2; a light-emitting layer 4 disposed on the hole transport layer 3; an electron transport layer 5 disposed on the light-emitting layer 4; and a cathode layer 6 disposed on the electron transport layer 5, wherein the light-emitting layer 4 includes the thermally activated delayed fluorescent (TADF) material.
According to an embodiment of the invention, in the electroluminescent device, the base layer is made of material including ITO; the hole injection layer is made of material including 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexaazatriphenylene; the hole transport layer 3 is made of material including 44,4′,4″-Tris(carbazol-9-yl)-triphenylamine (TCTA); the electron transport layer 5 is made of material including 1,3,5-tris(3-(3-pyridyl)phenyl)benzene (Tm3PyPB); and the cathode layer is made of material including lithium fluoride and aluminum.
Specifically, Compound 1, Compound 2, and Compound 3 are used as the light-emitting layers 4 to manufacture Device 100, Device 200, and Device 300, respectively, and performance of Device 100, Device 200, and Device 300 was measured. In each of Device 100, Device 200, and Device 300 is 2 nm, a thickness of each of the base layer 1 and the hole injection layer 2 is 2 nm, and a thickness of the hole transport layer 3 is 35 nm. The light-emitting layer 4 of Device 100, Device 200, and Device 300 includes 7% of Compound 1, Compound 2, and Compound 3, respectively, and has a thickness of 40 nm. A thickness of the electron transport layer 5 is 40 nm, and in the cathode 6, a thickness of lithium fluoride is 1 nm, and a thickness of aluminum is 100 nm.
The current-brightness-voltage characteristics of Device 100, Device 200, and Device 300 were further measured by a Keithley source measurement system (Keithley 2400 Sourcemeter, Keithley 2000 Currentmeter) with a calibrated silicon photodiode. The electroluminescence spectrum was measured by a French JY SPEX CCD3000 spectrometer. All measurements were conducted at room temperature under ambient atmosphere. The performance data of Device 100, Device 200, and Device 300 is shown in Table 2 below, and Device 100, Device 200, and Device 300 meet the performance requirements.
TABLE 1
Maximum current maximum external
Device efficiency (cd/A) CIEy quantum efficiency (%)
Device 100 86.7 0.25 34.1%
Device 200 77.5 0.25 30.8%
Device 300 64.3 0.25 28.9%
Accordingly, an embodiment of the present invention provides a thermally activated delayed fluorescence (TADF) material as a host of a green light-emitting guest, and using 100% of the internal quantum efficiency of the TADF material, a fluorescent device can achieve efficiency of a phosphorescent device, while solving the problems of excessively broad spectrum and long exciton life, thereby overcoming the problem of color gamut difference when directly using the TADF light-emitting material, such that blockade of UDC patents in phosphorescent heavy metal complex can be broken, and cost is significantly reduced. Therefore, a series of high-performance TADF organic light-emitting diodes (OLEDs) can be prepared by using the light-emitting materials provided by the present invention.
While the invention has been described by way of example and in terms of the preferred embodiments, it is to be understood that the invention is not limited to the disclosed embodiments. To the contrary, it is intended to cover various modifications and similar arrangements. Therefore, the scope of the appended claims should be accorded the broadest interpretation so as to encompass all such modifications and similar arrangements.

Claims (8)

What is claimed is:
1. An electroluminescent device, comprising:
a base layer;
a hole injection layer disposed on the base layer;
a hole transport layer disposed on the hole injection layer;
a light-emitting layer disposed on the hole transport layer;
an electron transport layer disposed on the light-emitting layer; and
a cathode layer disposed on the electron transport layer,
wherein the light-emitting layer comprises a thermally activated delayed fluorescent material, the thermally activated delayed fluorescent material comprises a compound composed of an acceptor A and a donor D, the compound having a following structural formula of Formula 1:

D-A Formula 1,
wherein the acceptor A is selected from any one of following structural formulas:
Figure US11380847-20220705-C00017
and the donor D has a following structural formula:
Figure US11380847-20220705-C00018
wherein the base layer is made of a material comprising ITO, the injection layer is made of a material comprising 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexaazabenzophenanthrene; the hole transport layer is made of a material comprising 4,4′,4″-tris(carbazole-9-yl)triphenylamine; the electron transport layer is made of a material comprising 1,3,5-tris(3-(3-pyridyl)phenyl)benzene(Tm3PyPB); and the cathode layer is made of a material comprising lithium fluoride and aluminum.
2. A method of preparing a thermally activated delayed fluorescent material, comprising the following steps:
Step S1: performing a reaction between a compound of A-X and a compound of D-H in a solution containing an alkali with catalyst at a first temperature for a first duration to obtain a reaction solution, wherein X is a halogen, A is selected from any one of the following structural formulas:
Figure US11380847-20220705-C00019
and D has a following structural formula:
Figure US11380847-20220705-C00020
Step S2: cooling the reaction solution to a second temperature to obtain a mixture; and
Step S3: separating the thermally activated delayed fluorescent material from the mixture, wherein the compound is composed of an acceptor A and a donor D, and the compound has a following structural formula of Formula 1:

D-A Formula 1.
3. The method of preparing the thermally activated delayed fluorescent material according to claim 2, wherein the first temperature is 120° C., and the first duration is 48 hours.
4. The method of preparing the thermally activated delayed fluorescent material according to claim 2, wherein the second temperature is room temperature.
5. The method of preparing a thermally activated delayed fluorescent material according to claim 2, wherein in the step S1, the solution containing the alkali is toluene, the alkali is sodium tert-butoxide, and the catalyst comprises acetic acid palladium and tri-tert-butylphosphine tetrafluoroborate.
6. The method of preparing the thermally activated delayed fluorescent material according to claim 2, wherein the step S2 further comprises extracting the reaction solution several times with dichloromethane and combining organic extracts to obtain the mixture.
7. The method of preparing the thermally activated delayed fluorescent material according to claim 2, wherein in the step S3, the separating is performed by column chromatography with an eluent of methylene chloride and n-hexane in a volume ratio of 1:1.
8. The method of preparing the thermally activated delayed fluorescent material according to claim 2, wherein the step S1 is performed under an inert environment.
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